Zobrazeno 1 - 10
of 25
pro vyhledávání: '"E Venkataswamy"'
Autor:
Shweta Mahalingam, Angela Devanboo, Avinash Pradhan, Ashwini Suravaparu, T. Sai Kiranmai, E. Venkataswamy, V. L. Ramprasad, Priya Kadam
Publikováno v:
The Journal of Obstetrics and Gynecology of India. 73:180-182
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61fa884d4378adc5383ec2ad427e6c99
https://doi.org/10.1007/s13224-022-01730-y
https://doi.org/10.1007/s13224-022-01730-y
Akademický článek
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Autor:
Shilpa Prabhudesai, Prashanth K Jayanna, Ashwini Nargund, Geeta V Patil Okaly, E Venkataswamy, Chandra Rao Juvva
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 7, Iss 7, Pp 1366-1371 (2013)
Background: Flow cytometry has come to occupy the vanguard of the high through put diagnostic techniques that have been used to differentiate between various chronic lymphoproliferative disorders (CLPD). However, economic considerations have created
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98f79184c83a12ab2ae73f3e70c9c2ac
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 55, Iss 4, Pp 574-577 (2012)
Acute promyelocytic leukemia (APL) is a subtype of acute myeloid leukemia (AML) in which abnormal promyelocytes predominate. APL is rare in children (approximately 10% of childhood AML) and is characterized by a higher incidence of hyperleukocytosis,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c01d8c26ce78c677bd3e3d1d7c0509f
http://www.ijpmonline.org/article.asp?issn=0377-4929
http://www.ijpmonline.org/article.asp?issn=0377-4929
Publikováno v:
International Journal of Human Genetics. 10:33-39
A majority of subjects with mental retardation and congenital anomalies cannot be classified under anyknown malformation syndromes. Major problems in understanding the mechanisms involved in the pr...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a372498be42da090e52edc357a5f06f
https://doi.org/10.1080/09723757.2010.11886082
https://doi.org/10.1080/09723757.2010.11886082
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
S A Gangoli, R Tejaswi, Shamir Rahman, Shilpa Prabhudesai, C T Satheesh, S Patil, Raghavendra M Rao, Diganta Hazarika, Radheshyam Naik, Tejaswini Bn, Ravi B Diwakar, S Kakara, Rashmita Sahoo, Vidya H Veldore, Subhrendu K. Pattanayak, S P Shashidhar, E Venkataswamy, N Krishnamoorthy, B S Ajai Kumar
Publikováno v:
Indian journal of cancer. 50(2)
Background: Epidermal growth factor receptor (EGFR) mutation plays a vital role in the prognosis of patients with lung cancer. However, there is a dearth of studies on EGFR mutation in Indian population. In this retrospective study conducted at a net
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1b5f5fc29d9ca1a21cd1932b29db780
https://pubmed.ncbi.nlm.nih.gov/23979197
https://pubmed.ncbi.nlm.nih.gov/23979197
Autor:
Rashmita Sahoo, V. Chitti Babu, S. M. Rao, Raghavendra M Rao, Ashwini R. Nargund, Bhagya S. Ajaikumar, E Venkataswamy, Gopal Krishna R. Dhondalay, Jayashree Kulkarni, V Vidya Harini, Geeta V Patil
Publikováno v:
Onkologie. 34(7)
Fluorescent in situ hybridization (FISH) equivocal results for Her-2/neu still pose a diagnostic dilemma in oncology practice. In this study, we evaluate if Her-2/neu mRNA expression is an alternative to FISH for detecting Her-2/neu positivity.Archiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1e76746c44d5e2e3e974b814b816c8d
https://pubmed.ncbi.nlm.nih.gov/21734421
https://pubmed.ncbi.nlm.nih.gov/21734421
Autor:
B S Ajai Kumar, Ashwini Nargund, V. Chitti Babu, V Vidya Harini, Rashmita Sahoo, Geeta V Patil Okaly, S. M. Rao, Raghavendra M Rao, E Venkataswamy
Publikováno v:
Lung cancer (Amsterdam, Netherlands). 73(3)
Epidermal growth factor receptor (EGFR) is one of the targeted molecular markers in many cancers including the lung malignancy. Genetic modifications such as deletions, insertions and Single Nucleotide Polymorphisms in the tyrosine kinase (TK) domain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44d02a722e5ce9b77407a67225ee0fe5
https://pubmed.ncbi.nlm.nih.gov/21996090
https://pubmed.ncbi.nlm.nih.gov/21996090
Autor:
Rashmita Sahoo, Shilpa Prabhudesai, Prasannakumari, Amit Verma, Ashwini R. Nargund, E Venkataswamy, Geeta V Patil, S. Patil, Basavalinga S. Ajaikumar, Rao J Chandra, Vidya H Veldore
Publikováno v:
Indian Journal of Human Genetics
Del(5)(q) is a common chromosomal abnormality with favourable prognosis in Myelodysplastic Syndrome (MDS) and Acute myeloid leukemia (AML). However, del(5)(q) is also seen rarely in Acute lymphoblastic leukemia (ALL) and its significance remains poor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92dc01de1d1e1070f9e7adf244906d09
https://doi.org/10.4103/0971-6866.108028
https://doi.org/10.4103/0971-6866.108028